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Zinc-promoted hydrohydrazination of terminal alkynes: An efficient domino synthesis of indoles
被引:152
|
作者
:
Alex, Karolin
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Alex, Karolin
[
1
]
Tillack, Annegret
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Tillack, Annegret
[
1
]
Schwarz, Nicolle
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Schwarz, Nicolle
[
1
]
Beller, Matthias
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
Beller, Matthias
[
1
]
机构
:
[1]
Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
来源
:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
|
2008年
/ 47卷
/ 12期
关键词
:
alkynes;
hydrohydrazinations;
indole;
zinc;
D O I
:
10.1002/anie.200703823
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
(Chemical Equation Presented) Indole click chemistry: The quest for better catalysts for the intermolecular hydrohydrazination to indoles leads to zinc salts. A simple one-pot synthesis forms indoles from arylhydrazines and terminal alkynes. The pharmacologically relevant indole building blocks are selectively formed in the presence of zinc triflate (Zn(OTf)2) or ZnCl 2 (see scheme). © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:2304 / 2307
页数:4
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